Jones Alicia M, Atkinson Joshua T, Silberg Jonathan J
Biosciences Department, Rice University, MS-140, 6100 Main Street, Houston, TX, 77005, USA.
Systems, Synthetic, and Physical Biology Graduate Program, Rice University, 6100 Main MS-180, Houston, TX, 77005, USA.
Methods Mol Biol. 2017;1498:295-308. doi: 10.1007/978-1-4939-6472-7_19.
Rearrangements that alter the order of a protein's sequence are used in the lab to study protein folding, improve activity, and build molecular switches. One of the simplest ways to rearrange a protein sequence is through random circular permutation, where native protein termini are linked together and new termini are created elsewhere through random backbone fission. Transposase mutagenesis has emerged as a simple way to generate libraries encoding different circularly permuted variants of proteins. With this approach, a synthetic transposon (called a permuteposon) is randomly inserted throughout a circularized gene to generate vectors that express different permuted variants of a protein. In this chapter, we outline the protocol for constructing combinatorial libraries of circularly permuted proteins using transposase mutagenesis, and we describe the different permuteposons that have been developed to facilitate library construction.
在实验室中,改变蛋白质序列顺序的重排被用于研究蛋白质折叠、提高活性以及构建分子开关。重排蛋白质序列最简单的方法之一是通过随机环化置换,即将天然蛋白质的末端连接在一起,并通过随机的主链断裂在其他位置产生新的末端。转座酶诱变已成为一种生成编码蛋白质不同环化置换变体文库的简单方法。通过这种方法,一个合成转座子(称为置换转座子)被随机插入到一个环化基因中,以产生表达蛋白质不同置换变体的载体。在本章中,我们概述了使用转座酶诱变构建环化置换蛋白质组合文库的方案,并描述了为便于文库构建而开发的不同置换转座子。